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Acta Paediatrica (Oslo, Norway : 1992)|July 16, 2014
Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome casesK Läer, M Vennemann, T Rothämel, et al.
Forensic Science International|September 6, 2005
DNA polymorphisms in the tyrosine hydroxylase and GNB3 genes: association with unexpected death from acute myocardial infarction and increased heart weightM Klintschar, D Stiller, P Schwaiger, et al.
International Journal of Legal Medicine|February 2, 2000
Nine STR markers plus amelogenin (AmpFlSTR Profiler Plus): a forensic study in an Austrian populationF Neuhuber, M Radacher, N Meisner, et al.
Rechtsmedizin (Berlin, Germany)|April 28, 2021
[Case report: death of a 2-year-old girl with postmortem diagnosis of a rare coronary artery vasculitis typical for Kawasaki syndrome]K Kanngießer, N Kono, J-T Suhren, et al.
Journal of Forensic Sciences|July 22, 1998
Genetic variation at the short tandem repeat loci HumvWA, HumFXIIIB, and HumFES/FPS in the Egyptian and Yemenian populationsM Klintschar, N al-Hammadi, T Lux, et al.
Obstetrics and Gynecology|October 8, 1999
Separation of sperm and vaginal cells with flow cytometry for DNA typing after sexual assaultW M Schoell, M Klintschar, R Mirhashemi, et al.
International Journal of Legal Medicine|February 9, 2021
Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS)J Kerz, P Schürmann, T Rothämel, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Evidence of fetal microchimerism in Hashimoto's thyroiditisM Klintschar, P Schwaiger, S Mannweiler, et al.
International Journal of Legal Medicine|February 5, 1999
Genetic variation and sequence studies of a highly variable short tandem repeat at the D17S976 locusM Klintschar, B Glock, E M Dauber, et al.
Forensic Science International|March 26, 2004
Persisting fetal microchimerism does not interfere with forensic Y-chromosome typingM Klintschar, P Schwaiger, S Regauer, et al.
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